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3 Human Nutritional Sciences, 4 Faculty of Medicine, and 5 Faculty of Pharmacy, University of Manitoba, Winnipeg, R3T 2N2 MB, Canada and 6 Assembly of Manitoba Chiefs, Winnipeg, R3C 0M6 MB, Canada
* To whom correspondence should be addressed. E-mail: hope.weiler{at}mcgill.ca.
| ABSTRACT |
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| Introduction |
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The 24-h recall method is the most frequently used approach in quantitatively assessing dietary intake in Aboriginal populations, including Canadian Aboriginals (1113). The 24-h recall is dependent on season and must be performed each season to reflect intake as regulated by food availability. This is an important consideration, because a number of traditional foods are high in calcium, but they are not consumed throughout the year. This also is true for vitamin D from consumption of milk products, fish, and fish liver oils. FFQ are designed to capture intake over an extended period of time that would reflect seasonal variations in food intake. A FFQ including traditional foods has been successfully used in Canadian Inuit populations (14) and American Native children (15). A FFQ reflecting the dietary practices of Aboriginal women in Manitoba was not available. Therefore, the objective of the First Nations Bone Health Study (FNBHS) was to accurately estimate dietary intake of calcium and vitamin D, by designing a culturally appropriate dietary survey instrument, and then determine whether disparities exist in dietary calcium, dietary vitamin D intake, and serological indicators of vitamin D sufficiency in a large cohort of Aboriginal and white women.
| Materials and Methods |
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Development and pretesting of the questionnaire.
The FFQ used in the Canadian Multicentre Osteoporosis Study (16), which is specific to calcium and vitamin D, was adapted to include traditional foods known to be either high or low in calcium, but already reported to be consumed in large enough quantities to contribute to dietary calcium intake (e.g., bannock bread at 84 mg/serving). The adapted FFQ was then tested for its content validity with respect to the nutritional habits of Aboriginal women
20 y, through one-on-one interviews with urban Aboriginal women (n = 8) and focus groups (15 women in 3 groups) and subsequently tested for reliability in another 8 Aboriginal women.
We decided that the survey would be used; however, it would be administered by an interviewer, because food models helped, measurements would be in standard household units (e.g., cups), and language barriers could be accommodated.
Validation of the FFQ. We used the 24-h recall method for assessing dietary intake and blood sampling to determine 25(OH)D concentrations. Participants completed the FFQ with the assistance of a registered dietitian, who subsequently conducted the 24-h recall interview. The assessments were repeated twice more at 2-wk intervals. The 24-h recall and FFQ intake data were entered into the NutriWatch nutrient analysis software program and totals for calcium and vitamin D were calculated and averaged. Dietary intakes of calcium and vitamin D were compared between the 24-h recall and FFQ on 3 different occasions for each participant. Further validation was done by comparing test results to serum 25(OH)D measured at the final visit at the end of October. The reliability of the FFQ and 24-h recall methods was examined by calculating the CV for calcium and vitamin D intakes.
Subjects. The study population consisted of urban Aboriginal, rural Aboriginal, and urban non-Aboriginal females (white). For the urban cohort, we used the Status Verification System files and the provincial (Manitoba Health) registry files to identify women residing at a Winnipeg address, to which a letter introducing the study had been mailed. For this study, urban was defined as when the subject lived within 50 km of the Winnipeg study center. Subjects who were pregnant or recently pregnant and those currently or recently breastfeeding (within 6 mo) were excluded. Rural recruitment focused on 2 Aboriginal communities, one from the northern Manitoba zone and the other from the south. Local community interviewers were identified from each of these communities and they completed interviewer-training sessions. Random samples were drawn from the band lists.
Clinical assessment. Vitamin D status was assessed from serum 25(OH)D concentrations measured using RIA (Diasorin) at the Winnipeg Health Sciences Centre, where the inter-assay CV was 613%. The assay measures both ergocalciferol (D2) and cholecalciferol (D3).
Body weight was measured to the nearest 0.5 lb with a portable digital scale (Tanita TBF-612) and subsequently converted to kg. Height was measured to the nearest 0.1 cm with a Harpenden pocket stadiometer (Holtain).
Statistical analysis.
Normality of the data were tested using the method of Kolmogorov and Smirnov. Data that were not normally distributed [all data from FFQ and 25(OH)D] were log transformed prior to analysis. Factorial ANOVA was used to identify the main effects of ethnicity (Urban white, Urban Aboriginal, and Rural Aboriginal) and age groups were defined using the dietary recommended intake (DRI) ranges. The age ranges for the groups were divided into women 2550 y and
51 y. The DRI values for women 2550 y are 1000 mg calcium and 5 µg vitamin D. For women
51 y, the DRI for calcium is 1200 mg. The requirement for vitamin D is 10 µg for 51- to 70-y-old women and 15 µg for those >70 y; however, because there were few women over 70 y, the groups were combined. Post-hoc testing with least square means and Bonferroni correction was used when a main effect of ethnic group was identified, or if an ethnic group by age-group interaction was identified. Simple linear regression was used to examine the relation between vitamin D intake and serum 25(OH)D concentrations. Differences with P < 0.05 were considered significant.
| Results |
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The women in this study were between 25 and 76 y of age. By design, there were no differences in age among the ethnic cohorts (Table 1). There was a main effect of age (P < 0.05) on body weight, with younger women weighing more than the older women (79.2 ± 19.2 vs. 77.2 ± 15.6 kg). There was also a main effect of both ethnicity (P < 0.03) and age (P < 0.0001) on height. Rural Aboriginal women were taller than urban Aboriginal women and white women were intermediate. Younger women were taller than older women.
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There was a main effect (P < 0.001) of ethnic cohort on vitamin D status as assessed by serum 25(OH)D. Women in the rural and urban Aboriginal group had lower (P < 0.0004) concentrations than urban white women. There was also a main effect (P < 0.03) of age group. Older women had higher serum 25(OH)D concentrations than younger women. Dietary vitamin D intake and 25(OH)D were significantly related only in the white women (Fig. 2).
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| Discussion |
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The values for dietary calcium intake reported herein support other Canadian reports. Aboriginal women from Northern Manitoba Cree Communities have very low intakes of calcium (288476 g/d) (13). Similarly, 58% of Ojibwa-Cree in Northern Ontario women have low calcium intakes; mean intakes range from 547 mg/d in women 2049 y of age to 634 g/d in those >49 y (12). As many as 25% (3), and up to 70% (5), of white Canadian women do not achieve dietary intakes in line with the 1990 recommended calcium intakes of 700800 mg/d (17). Newly published data from the Canadian Community Health Survey of over 30,000 Canadians show that women consume, on average, 1.6 servings of milk per day, which provides
480 mg calcium. This is similar to the calcium contribution from milk seen in our study, which was 465 mg, well below the DRI of 10001200 mg/d (18) for adult women between 19 and 65 y of age. Only a minority of women in this study had an intake of calcium above the AI value.
In contrast to dietary calcium intake, more women met the AI for vitamin D. However, dietary intake of vitamin D was related to vitamin D status only in the white women of this study. The lack of an association between diet and vitamin D status in the Aboriginal women was not likely due to sampling in different seasons, because the proportion of white women studied in winter, when vitamin D status is most reflective of diet, was 55.5%, vs. 73% of Aboriginal women.
According to the DRI Committee, a serum 25(OH)D concentration <37.5 nmol/L is indicative of vitamin D deficiency (18). Using this cutoff, 32% of rural Aboriginal women, 30.4% of urban Aboriginal women, and 18.6% of urban white women in this study are defined as vitamin D deficient. A circulating 25(OH)D of 75 nmol/L is more recently thought to represent optimal status (19). Given this definition, 96% of rural Aboriginal, 84% of urban Aboriginal, and 62% of white women are below optimal vitamin D status. To obtain a serum 25(OH)D concentration of 75 nmol/L, 2025 µg vitamin D would be required daily (19).
Regardless of the values of serum 25(OH)D used to indicate vitamin D deficiency or optimal vitamin D status, it is clear that vitamin D deficiency is common in Aboriginal women, possibly due to the predominance of residence in more extreme northern latitudes, skin pigmentation, or lifestyle. In Northern Manitoba (49°N), 76% of women have serum 25(OH)D concentrations in the deficient range (9). Similarly, in other predominantly white northern populations, 34% of women (2789 y) living in Calgary (51°N) have low vitamin D status in at least 1 season (6). Even in the Toronto region (43°N), the prevalence of vitamin D deficiency is reported to be 14.8% in white women and 25.6% in nonwhite nonblack women (7). Dietary or supplemental vitamin D intakes at levels similar to the AI value of 5 µg/d did not improve deficiency rates in this population (18). Cutaneous synthesis of vitamin D in these regions is thought to be limited to April through September (20), placing many Canadians at risk for vitamin D deficiency and potentially limited bone mass or metabolism.
A recent report on Native American women suggests they have higher bone mass than white women but that bone mass is more readily lost during postmenopausal years (21). Vitamin D status and BMI, both of which are also health concerns in Canadian Aboriginal women (9,22), accounted for 70% of the variance in bone mass in lumbar spine and femoral neck (21). More rapid loss of bone and continued high bone turnover in aging might represent greater risk for fracture than suggested by bone mineral density, T-, and Z-scores (23). High bone turnover may be associated with inadequate dietary calcium and deficiency of vitamin D. Although BMI was not related to vitamin D status in this study, all cohorts and age groups were, on average, either overweight (25.029.9 kg/m2) or obese class I (30.034.9 kg/m2). Whether Aboriginal women in Manitoba have a higher fracture rate (2) as a result of inadequate dietary calcium, vitamin D, and vitamin D status as related to BMI requires further investigation.
The study is not without its limitations. The FFQ validation portion of the study suggests that the FFQ could be used to estimate intake of calcium and vitamin D in this population. It was not possible to accurately validate the FFQ because the number of participants in this questionnaire validation portion of the study was low. To further validate the FFQ results, blood sampling was done at the final study visit at the end of October, when 25(OH)D concentrations would be more reflective of diet than UVB exposure in Manitoba. Considering that the half-life of 25(OH)D is between 10 d and 3 wk (24), October may not have been late enough to eliminate the effect of endogenous synthesis; however, both the 24-h recall and FFQ yielded a vitamin D intake that was positively related to vitamin D status. Lastly, it would have been optimal to collect multiple 24-h recalls throughout the year, as the comparison method, but this was not feasible.
In summary, dietary calcium intake was below recommendations for both Aboriginal and white women. Despite intakes of vitamin D consistent with the adequate intake, vitamin D deficiency was evident in all women, regardless of age or ethnic grouping. Milk and margarine were key sources of vitamin D in this study and this underscores the importance of Canada's fortification policy, which mandates these 2 staple foods be fortified with vitamin D. Further exploration of how to remedy vitamin D deficiency in Aboriginal and white women will help to provide data from which to revise vitamin D fortification policy.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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2 In Canada, the terms Aboriginal or Native are used to refer to "Indians", and includes First Nations, Metis, and Inuit peoples. First Nations are Aboriginal peoples signatory to Treaties and/or recognized by the federal government as a fiduciary responsibility. This article reports on data derived exclusively from First Nations populations, which represent the large majority of Aboriginal persons living in Canada. ![]()
7 Abbreviations used: AI, adequate intake; DRI, dietary recommended intake; FNBHS, First Nations Bone Health Study; [25(OH)D], 25-hydroxyvitamin D. ![]()
Manuscript received 14 June 2006. Initial review completed 9 August 2006. Revision accepted 17 November 2006.
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